In:
Movement Disorders Clinical Practice, Wiley, Vol. 5, No. 1 ( 2018-01), p. 31-38
Abstract:
Psychosis is among the most disabling complications of Parkinson's disease ( PD ). The chronicity of PD psychosis remains understudied, and the relative importance of dopaminergic therapy versus the disease process itself in engendering psychosis remains unclear. The objective of this study was to examine pharmacologic and motoric correlates of PD psychosis onset and remission in a longitudinally monitored PD cohort. Methods We analyzed data from 165 participants enrolled in a longitudinal PD study through the Morris K. Udall Parkinson's Disease Research Center of Excellence at Johns Hopkins University. Evaluations included formal psychiatric assessment and were conducted at 2‐year intervals. Regression with generalized estimated equations was used to produce unadjusted and adjusted estimates for time‐varying longitudinal associations between psychosis and putative risk factors. Results Sixty‐two participants (37.6%) were diagnosed with psychosis during at least 1 evaluation. Of 49 participants with psychosis who were followed over multiple evaluations, 13 (26.5%) demonstrated remission despite a significant increase in Hoehn & Yahr stage ( P = 0.009); 2 of these individuals later relapsed. Multivariable regression with generalized estimated equations identified dementia diagnosis, akinesia‐rigidity, anticholinergic usage, and levodopa‐carbidopa dose as significantly associated with psychosis, whereas disease duration was not. A subanalysis of 30 incident psychosis cases suggested that the dopamine agonist dose was lowered after psychosis onset with a compensatory increase in the levodopa‐carbidopa dosage. Conclusion The current findings suggest that, in the context of standard therapy, PD ‐related psychotic disorder can remit at a frequency of approximately 27%. In addition, akinetic‐rigid motor impairment was more strongly associated with psychosis than disease duration, independent of cognitive impairment and medications.
Type of Medium:
Online Resource
ISSN:
2330-1619
,
2330-1619
DOI:
10.1002/mdc3.2018.5.issue-1
Language:
English
Publisher:
Wiley
Publication Date:
2018
detail.hit.zdb_id:
2772809-2
